Associate Principal QA Specialist, QA Technical
Associate Principal QA Specialist, QA Technical

Associate Principal QA Specialist, QA Technical

Slough Full-Time No home office possible
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At a Glance

  • Tasks: Support QA compliance initiatives and manage quality records in a dynamic environment.
  • Company: Join a leading company in the pharmaceutical sector, committed to quality and innovation.
  • Benefits: Enjoy competitive pay, potential remote work options, and a supportive team culture.
  • Why this job: Be part of a mission-driven team that values quality and continuous improvement.
  • Qualifications: Bachelor's degree in a scientific field and advanced QA/QC experience required.
  • Other info: Initial onsite work with flexible remote options after training.

Mid-Senior level £27.00/hr – £32.00/hr United Kingdom Slough, England, United Kingdom

45 days ago

Associate Principal QA Specialist, QA Technical

Location: Slough (initially onsite with possibility of 1-2 days working from home thereafter)

Schedule: Standard Office Hours

Duration: 12-Month Contract

Pay: £27-32/hr

Job Responsibilities

In this role, you will support Quality Assurance (QA) compliance initiatives across site operations. Key responsibilities include:

• Overseeing the review, approval, and management of quality records, including deviations, CAPAs, change controls, and investigations.
• Collaborating with cross-functional teams to resolve compliance issues and promote continuous improvement.
• Providing subject matter expertise (SME) on GMP processes, maintaining audit readiness and regulatory compliance.
• Coaching teams to uphold and enhance a culture of quality.

Essential Duties and Job Functions

• Provide direct support and approval of quality documentation (e.g., Deviations, CAPAs, Change Controls, OOS).
• Manage critical compliance issues through site QMS processes, ensuring timely escalation and resolution.
• Actively identify and contribute to quality and process improvement initiatives.
• Serve as QA SME in governance forums and cross-functional project teams.
• Support manufacturing operations during regular and off-hours as needed.
• Maintain ongoing audit readiness in alignment with regulatory and internal standards.
• Participate in development and enhancement of quality systems and documentation.
• Coach and mentor operational staff on cGMP and quality best practices.
• Execute additional duties as assigned by QA leadership.

Knowledge & Skills

• Strong decision-making and problem-solving abilities.
• Solid understanding of GMP compliance and quality systems.
• Effective communication and interpersonal skills to influence and guide stakeholders.
• Strong attention to detail and organizational skills.
• Continuous improvement mindset with experience in quality/process optimization.
• Ability to manage multiple priorities and meet tight deadlines.
• Comfortable working in cross-functional teams and high-paced environments.

Education & Experience

• Education: Bachelor\’s degree in a scientific discipline (required).
• Experience: Advanced-level experience in QA or QC.
• Prior experience reviewing and approving GMP documentation (e.g., deviations, CAPAs, change controls, OOS) is essential.
• Familiarity with pharmaceutical/biotech regulatory requirements preferred.

…

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Associate Principal QA Specialist, QA Technical employer: QA

As an Associate Principal QA Specialist in Slough, you will join a dynamic team that prioritises quality and compliance within a supportive work environment. The company fosters a culture of continuous improvement and offers opportunities for professional growth, including coaching and mentoring roles, while also providing flexibility with the option to work from home after initial onboarding. With competitive pay and a commitment to maintaining high standards, this role is ideal for those seeking meaningful contributions in the pharmaceutical sector.
Q

Contact Detail:

QA Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Associate Principal QA Specialist, QA Technical

✨Tip Number 1

Familiarise yourself with the latest GMP regulations and quality systems. Being well-versed in these areas will not only boost your confidence during interviews but also demonstrate your commitment to maintaining compliance.

✨Tip Number 2

Network with professionals in the QA field, especially those who have experience in pharmaceutical or biotech industries. Engaging with them can provide insights into the role and may even lead to referrals.

✨Tip Number 3

Prepare to discuss specific examples of how you've contributed to quality improvement initiatives in your previous roles. Highlighting your hands-on experience will set you apart from other candidates.

✨Tip Number 4

Showcase your ability to work in cross-functional teams by preparing examples of successful collaborations. This is crucial for the Associate Principal QA Specialist role, as you'll need to influence and guide various stakeholders.

We think you need these skills to ace Associate Principal QA Specialist, QA Technical

GMP Compliance
Quality Management Systems (QMS)
Deviation Management
CAPA Management
Change Control Processes
Investigative Skills
Regulatory Compliance Knowledge
Coaching and Mentoring
Cross-Functional Collaboration
Problem-Solving Skills
Attention to Detail
Organisational Skills
Continuous Improvement Mindset
Effective Communication Skills
Ability to Manage Multiple Priorities

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in Quality Assurance and compliance. Emphasise your familiarity with GMP processes and any specific achievements in quality improvement initiatives.

Craft a Strong Cover Letter: Write a cover letter that directly addresses the job responsibilities listed in the description. Use specific examples from your past experience to demonstrate how you meet the essential duties and skills required for the role.

Highlight Relevant Skills: In your application, clearly outline your decision-making and problem-solving abilities. Mention your experience with quality documentation and your ability to work in cross-functional teams, as these are key aspects of the role.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects attention to detail, which is crucial for a QA role.

How to prepare for a job interview at QA

✨Showcase Your QA Knowledge

Make sure to brush up on your understanding of GMP compliance and quality systems. Be prepared to discuss specific examples from your past experience where you successfully managed quality documentation or resolved compliance issues.

✨Demonstrate Problem-Solving Skills

During the interview, highlight your decision-making and problem-solving abilities. Prepare to share instances where you identified critical compliance issues and how you contributed to their resolution.

✨Emphasise Team Collaboration

Since this role involves working with cross-functional teams, be ready to discuss your experience in collaborating with others. Share examples of how you influenced stakeholders and promoted a culture of quality within your team.

✨Prepare for Technical Questions

Expect technical questions related to quality assurance processes, such as CAPAs and change controls. Familiarise yourself with common scenarios and best practices to demonstrate your expertise and readiness for the role.

Associate Principal QA Specialist, QA Technical
QA
Location: Slough
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Q
  • Associate Principal QA Specialist, QA Technical

    Slough
    Full-Time
  • Q

    QA

    200-500
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